Prediagnostic serum calcium concentrations and risk of colorectal cancer development in 2 large European prospective cohorts

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  • Nena Karavasiloglou
  • David J. Hughes
  • Neil Murphy
  • Lutz Schomburg
  • Qian Sun
  • Vartiter Seher
  • Sabine Rohrmann
  • Elisabete Weiderpass
  • Anja Olsen
  • Kim Overvad
  • Marie Christine Boutron-Ruault
  • Francesca Romana Mancini
  • Yahya Mahamat-Saleh
  • Rudolf Kaaks
  • Tilman Kuhn
  • Matthias B. Schulze
  • Rosario Tumino
  • Salvatore Panico
  • Giovanna Masala
  • Valeria Pala
  • Carlotta Sacerdote
  • Jeroen W.G. Derksen
  • Guri Skeie
  • Anette Hjartåker
  • Cristina Lasheras
  • Antonio Agudo
  • Maria José Sánchez
  • Maria Dolores Chirlaque
  • Eva Ardanaz
  • Pilar Amiano
  • Bethany Van Guelpen
  • Björn Gylling
  • Kathryn E. Bradbury
  • Keren Papier
  • Heinz Freisling
  • Elom K. Aglago
  • Amanda J. Cross
  • Elio Riboli
  • Dagfinn Aune
  • Marc J. Gunter
  • Mazda Jenab
Background
Higher dietary calcium consumption is associated with lower colorectal cancer (CRC) risk. However, little data are available on the association between circulating calcium concentrations and CRC risk.

Objectives
To explore the association between circulating calcium concentrations and CRC risk using data from 2 large European prospective cohort studies.

Methods
Conditional logistic regression models were used to calculate multivariable-adjusted ORs and 95% CIs in case-control studies nested within the European Prospective Investigation into Cancer and Nutrition (EPIC; n-cases = 947, n-controls = 947) and the UK Biobank (UK-BB; n-cases = 2759, n-controls = 12,021) cohorts.

Results
In EPIC, nonalbumin-adjusted total serum calcium (a proxy of free calcium) was not associated with CRC (OR: 0.94; 95% CI: 0.85, 1.03; modeled as continuous variable, per 1 mg/dL increase), colon cancer (OR: 0.93; 95% CI: 0.82, 1.05) or rectal cancer (OR: 1.01; 95% CI: 0.84, 1.20) risk in the multivariable adjusted model. In the UK-BB, serum ionized calcium (free calcium, most active form) was inversely associated with the risk of CRC (OR: 0.85; 95% CI: 0.76, 0.95; per 1 mg/dL) and colon cancer (OR: 0.78; 95% CI: 0.68, 0.90), but not rectal cancer (OR: 1.02; 95% CI: 0.83, 1.24) in multivariable adjusted models. Meta-analysis of EPIC and UK-BB CRC risk estimates showed an inverse risk association for CRC in the multivariable adjusted model (OR: 0.90; 95%CI: 0.84, 0.97). In analyses by quintiles, in both cohorts, higher levels of serum calcium were associated with reduced CRC risk (EPIC: ORQ5vs.Q1: 0.69; 95% CI: 0.47, 1.00; P-trend = 0.03; UK-BB: ORQ5vs.Q1: 0.82; 95% CI: 0.72, 0.94; P-trend < 0.01). Analyses by anatomical subsite showed an inverse cancer risk association in the colon (EPIC: ORQ5vs.Q1: 0.63, 95% CI: 0.39, 1.02; P-trend = 0.05; UK-BB: ORQ5vs.Q1: 0.75; 95% CI: 0.64, 0.88; P-trend < 0.01) but not the rectum.

Conclusions
In UK-BB, higher serum ionized calcium levels were inversely associated with CRC, but the risk was restricted to the colon. Total serum calcium showed a null association in EPIC. Additional prospective studies in other populations are needed to better investigate these associations.
OriginalsprogEngelsk
BogserieAmerican Journal of Clinical Nutrition
Vol/bind117
Udgave nummer1
Sider (fra-til)33-45
Antal sider13
ISSN0002-9165
DOI
StatusUdgivet - 2023

Bibliografisk note

Funding Information:
Part of the work reported in this paper was undertaken while NK was hosted by the International Agency for Research on Cancer and funded by the John Latsis Public Benefit Foundation and the International Agency for Research on Cancer . The rest of the work was conducted while she was funded by Krebsforschung Schweiz under Grant KFS-4114-02-2017 to SR. Funding for this study was also provided by the Health Research Board of Ireland project grants and HRA-POR/2013/397 (to DJH). Research and analytical work in the lab of LS is supported by the Deutsche Forschungsgemeinschaft (DFG) , Research Unit FOR-2558 “TraceAge” (Scho 849/6-1). KEB is supported by a Sir Charles Hercus Health Research Fellowship from the Health Research Council of New Zealand. KP is supported by Cancer Research UK and the Wellcome Trust Our Planet Our Health (Livestock, Environment and People). The coordination of EPIC is financially supported by International Agency for Research on Cancer (IARC) and also by the Department of Epidemiology and Biostatistics, School of Public Health, Imperial College London which has additional infrastructure support provided by the NIHR Imperial Biomedical Research Centre . The EPIC-Norfolk study (DOI 10.22025/2019.10.105.00004) has received funding from the Medical Research Council (MR/N003284/1 and MC-UU_12015/1) and Cancer Research UK (C864/A14136). The national EPIC cohorts are supported by: Danish Cancer Society (Denmark); Ligue Contre le Cancer, Institut Gustave Roussy, Mutuelle Générale de l’Education Nationale, Institut National de la Santé et de la Recherche Médicale (INSERM) (France); German Cancer Aid, German Cancer Research Center (DKFZ), German Institute of Human Nutrition Potsdam-Rehbruecke (DIfE), Federal Ministry of Education and Research (BMBF) (Germany); Associazione Italiana per la Ricerca sul Cancro-AIRC-Italy, Compagnia di SanPaolo and National Research Council (Italy); Dutch Ministry of Public Health, Welfare and Sports (VWS), Netherlands Cancer Registry (NKR), LK Research Funds, Dutch Prevention Funds, Dutch ZON (Zorg Onderzoek Nederland), World Cancer Research Fund, Statistics Netherlands (The Netherlands); Health Research Fund (FIS) - Instituto de Salud Carlos III (ISCIII), Regional Governments of Andalucía, Asturias, Basque Country, Murcia and Navarra, and the Catalan Institute of Oncology - ICO (Spain); Swedish Cancer Society, Swedish Research Council and Region Skåne and Region Västerbotten (Sweden); Cancer Research UK (14136 to EPIC-Norfolk; C8221/A29017 to EPIC-Oxford), Medical Research Council (1000143 to EPIC-Norfolk; MR/M012190/1 to EPIC-Oxford) (United Kingdom). None of the funding entities had any role in the design, implementation, analysis, or interpretation of the study findings.

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